Variant (rsID / SNP)

rs12586792

rs12586792 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR4Q2. Location: chromosome 14, position 20,470,903. The table records no clinical significance for this variant.

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Reference-table entries

OR4Q2Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 14:20470903
HGVS: NR_145508.1,n.683T>C
Allele change: Missense_F194S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.